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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Role of Menstrual Bleeding Assessments in Sickle Cell Clinics

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Innate immune dysregulation in monocytes in sickle cell disease

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Revisiting acute chest syndrome (ACS) associated with sickle cell disease (SCD) vaso-occlusive pain episodes (VOE): Insight from a prospective, multicenter Phase-3 randomized controlled trial

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Clinical and laboratory findings in adults with sickle cell disease which increase risk for severe acute chest syndrome

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Application and challenges of the sickle cell outcome grading system (SCOGS) for classifying acute chest syndrome severity

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Exercise capacity and oxygen saturation on six-minute walk testing relate to markers of organ dysfunction in adults with sickle cell disease

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Christine Briscoe 12/15/25 Christine Briscoe 12/15/25

Clinical and laboratory findings in adults with sickle cell disease which increase risk for severe acute chest syndrome

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Sickle cell disease trials redefined: Toward unified clinical endpoints through international consensus

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Qualitative interviews exploring the patient experience of fatigue in individuals with sickle cell disease (SCD), thalassemia, and pyruvate kinase (PK) deficiency

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Explainable AI-based prediction of chronic kidney disease as a long-term outcome of sickle cell disease in a large, multi-site observational data cohort

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Trust and relationships between people with sickle cell disease and healthcare professionals: Regional comparisons from the listen survey

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Evaluating the efficacy of brief neurocognitive assessments in adults and adolescents with sickle cell disease

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Financial and clinical implications of xromi as a new commercial liquid formulation of hydroxyurea

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Reclaiming the clinical social work role: A call for reform in sickle cell disease psychosocial care

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Describing the feasibility and acceptability of an electronic adherence monitor to measure hydroxyurea adherence among youth with sickle cell disease

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Cost-effectiveness of hydroxyurea for children with sickle cell disease in sub-saharan Africa: A discrete event simulation model to inform policy and government planning

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Baseline data from the prioritizing utilization and safety of hydroxyurea using precision in Africa (PUSHUP) trial

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Development of the sickle cell outcome grading system (SCOGS), a novel classification system for sickle cell disease severity

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Burnout in sickle cell disease-focused hematology-oncology trained providers: A national cross-sectional study

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Research Christine Briscoe 12/15/25 Research Christine Briscoe 12/15/25

Social isolation and patient-reported and healthcare utilization in adults with sickle cell disease

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